Hollow carbon fiber and production method

ABSTRACT

Production of hollow carbon fibers and hollow carbon particles includes baking and carbonization of polymer particles having a specified volume after deformation. A metal-deposited carbon fiber with metal deposited inside and/or outside the hollow carbon fiber is applicable to electron discharge devices. The thickness and crystallinity of the graphite layer can be freely controlled. Since almost no by-product is generated, separation and refining using a solvent is not required. A hollow carbon particle of desired shape can be produced at a high yield rate. The hollow carbon fiber represented by a carbon nano-tube can be controlled in such a way that a low resistance and uniform shape are provided so that there is an increase in the amount of electrons discharged from the hollow carbon fiber. Use of this hollow carbon fiber as an electron discharge source provides an excellent electron discharge device characterized by stable pixels.

This application is a Divisional application of application Ser. No.09/984,157, filed Oct. 29, 2001, the contents of which are incorporatedherein by reference in their entirety.

BACKGROUND OF THE INVENTION

The present invention relates to a hollow carbon fiber, a hollow carbonparticle, a production method thereof, and composite of the fiber andresin.

The hollow carbon fiber represented by a carbon nano-tube is several nmto several hundred nm in diameter and several nm to several dozen nm inlength, and the wall thereof is cylindrical in form and is made ofseveral to several dozen graphite walls (layers).

Such a hollow carbon fiber has attracted attention for such conspicuouscharacteristics as mechanical strength, hydrogen storage properties andelectric field discharge properties, and studies have been made on itspractical application.

Japanese Patent NO. 2845675 discloses a method in which carbon iscoagulated subsequent to its evaporation by arc discharge in an inactiveatmosphere; Japanese Application Patent Laid-Open Publication NO.109310/2000 discloses a method in which at least one of X-rays,microwaves and ultrasonic waves are applied to carbon material including—C° C— and/or —C═C—; and Japanese Application Patent Laid-OpenPublication NO. 95509/2000 discloses a method wherein a carbon nano-tubeis made to grow by contact between carbon vapor and a non-magnetictransition metal.

In any of these production methods, however, the yield of the intendedcarbon nano-tube is low, and the by-product of carbonaceous materialsimilar to carbon black and amorphous carbon cannot be avoided. When ametallic catalyst is used, it is necessary to refine the reactionproducts, and a metallic catalyst cannot be removed completely byrefining, with the result that the aforementioned hydrogen storageproperties and electric field discharge properties are reduced. Suchdisadvantages cannot be avoided in the prior art.

Further, the aforementioned production methods are practically incapableof controlling the number of wall layers, the diameter and the length ofthe hollow carbon tube represented by a carbon nano-tube. It has beenvery difficult to attain a uniform shape and uniform characteristics.

A hollow carbon particle represented by fullerene is several nm toseveral hundred nm in diameter, and the wall comprises several nm toseveral dozen graphite layers, including a five-membered ring orseven-membered ring.

Hollow carbon particles have attracted attention for such conspicuouscharacteristics as mechanical strength, hydrogen storage properties andelectric field discharge properties, and studies have been made on itspractical application. In the conventional method of its production,carbon is coagulated subsequent to its evaporation by arc discharge inan inactive atmosphere, and it is then separated and refined.

However, the yield of fullerene is low, and the by-product ofcarbonaceous material similar to carbon black and amorphous carboncannot be avoided. Further, separation and refining using a solvent,such as benzene, are essential, and a remarkable reduction inproductivity has been unavoidable.

Further, the aforementioned production methods are practically incapableof controlling the number of wall layers, the diameter and the length ofthe hollow carbon particles represented by fullerene.

SUMMARY OF THE INVENTION

An object of the present invention is to solve the problems involved inthe aforementioned known method of production of a hollow carbon fiberrepresented by a carbon nano-tube obtained therefrom, and hollow carbonparticles.

The present invention provides a method of manufacture of a hollowcarbon fiber and a hollow carbon particle, which allows the number ofwall layers, the diameter and the length of the hollow carbon particlesto be controlled, and ensures a uniform shape and uniformcharacteristics.

What is more, the present invention provides a hollow carbon fiber andits method of production, characterized by comparatively easy massproduction, since it does not use a metallic catalyst; hence, it doesnot require a step of refining and elimination thereof.

The present invention also provides a hollow carbon fiber and its methodof production, characterized by comparatively easy mass production withalmost no generation of by-products, separation or refining by asolvent.

The following is a summary of aspects of the present invention:

(1) A method of production of a hollow carbon fiber comprising a step ofbaking and carbonization of polymer particles having a volume of 100 mm³or smaller after deforming.

(2) A method of production of a hollow carbon fiber according to theaforementioned aspect (1), characterized by deforming the aforementionedpolymer particles by heating.

(3) A method of production of a hollow carbon fiber according to theaforementioned aspect (1) characterized by deforming polymer particleswith mechanical force.

(4) A method of production of a hollow carbon fiber according to theaforementioned aspect 1, characterized by deforming polymer particlesusing irradiation of electromagnetic waves.

(5) A method of production of a hollow carbon fiber according to theaforementioned aspect (1), characterized by deforming polymer particlesby any one or a combination of the methods described according to theaforementioned aspects (2) to (4).

(6) A method of production of a hollow carbon fiber according to theaforementioned aspect (1), characterized in the fact that the diameterof a polymer particle is 5 to 5000 times that of a hollow carbon fiberas a final product.

(7) A method of production of a hollow carbon fiber according to aspect(1), characterized in the fact that one or both ends of the fiber areclosed.

(8) A method of production of a hollow carbon fiber according to aspect(1), characterized in the fact that the aspect ratio (length/diameter)of the fiber is 1 or more.

(9) A method of production of a hollow carbon fiber according to aspect(1), characterized in that the diameter and length of a fiber arecontrolled by the volume of polymer particles.

(10) A method of production of a hollow carbon fiber according to aspect(1), characterized by a step of producing polymer particles by acombination of polymers disappearing due to thermal decomposition andcarbon precursor polymers.

(11) A method of production of a hollow-carbon fiber according to aspect(10), characterized by a step of producing a micro-capsule from polymersdisappearing due to thermal decomposition and carbon precursor polymers,and baking the aforementioned micro-capsule subsequent to melting andspinning.

(12) A method of production of a hollow carbon fiber according to aspect(10), characterized in the fact that the difference between thesoftening temperature of polymers disappearing due to thermaldecomposition and that of carbon precursor polymers does not exceed 100degrees Celsius.

(13) A method of production of a hollow carbon fiber according toaspects (10) or (11), characterized in the fact that the ratio betweeninner and outer diameters of the aforementioned hollow carbon fiber iscontrolled by a ratio of the thickness between the layer of polymersdisappearing due to thermal decomposition and that of carbon precursorpolymers.

(14) A method of production of a hollow carbon fiber according toaspects (10) or (11), characterized in the fact that the number oflayers of the aforementioned hollow carbon fiber is controlled by aratio of the thickness between the layer of polymers disappearing due tothermal decomposition and that of carbon precursor polymers.

(15) A method of production of a hollow carbon fiber according toaspects (10) or (11), characterized by using polymers wherein theresidual carbon percentage of polymers disappearing due to thermaldecomposition does not exceed 10 percent by weight and that of carbonprecursor polymers does not exceed 15 percent by weight.

(16) A method of production of a hollow carbon fiber according to aspect(11), characterized in the fact that the aforementioned micro-capsulesare prepared by an interfacial chemical technique.

(17) A method of production of a hollow carbon fiber according to aspect(11), characterized in the fact that the aforementioned micro-capsulesare prepared by seed polymerization.

(18) A method of production of a hollow carbon fiber according to aspect(11), characterized in the fact that the aforementioned carbon precursorpolymers are formed of a monomer comprising radically polymerizablegroups.

(19) A method of production of a hollow carbon fiber according to aspect(18), characterized in the fact that the aforementioned carbon precursorpolymer has units formed of acrylonitrile monomers contained inpolymers.

(20) A method of production of a hollow carbon fiber according to aspect(11), characterized in the fact that the aforementioned polymerdisappearing due to thermal decomposition is formed of a monomercomprising a radically polymerizable group.

(21) A method of production of a hollow carbon fiber according to aspect(11), characterized in the fact that a polymer disappearing due tothermal decomposition and a carbon precursor polymer are formed of amonomer comprising radically polymerizable groups, and compound whereincarbon remains as a major component in the process of carbonization isused as a polymerization initiator.

(22) A hollow carbon fiber according to aspect (1), characterized in thefact that the polymer particles each have a prescribed volume.

(23) A hollow carbon fiber according to any one of aspects (1) to (12)and (16) to (22), comprising a hollow member formed of a polymerdisappearing due to thermal decomposition and a carbon shell formed of acarbon precursor polymer.

(24) A composite of a hollow carbon fiber according to aspect (23) and aresin.

(25) A hollow carbon fiber characterized in the fact that the content ofmetal and a metallic compound does not exceed 1 percent by weight.

(26) A method of production of a hollow carbon fiber characterized inthe fact that the content of metal and a metallic compound does notexceed 1 percent by weight, where no metal or metallic compound is usedin the steps of production.

(27) A method of production of a hollow carbon fiber characterized inthe fact that the content of metal and a metallic compound does notexceed 1 percent by weight, where no metal or metallic compound iseliminated or refined in a step of the production.

(28) A hollow carbon fiber according to aspect (25) comprising a hollowmember formed of a polymer disappearing due to thermal decomposition andcarbon shells formed of a carbon precursor polymer.

(29) A method of production of a hollow carbon fiber according toaspects (26) or (27), characterized in the fact that the aforementionedhollow carbon fiber is produced by a combination of polymersdisappearing due to thermal decomposition and carbon precursor polymers.

(30) A method of production of a hollow carbon fiber according to aspect(29), characterized by a step of producing a micro-capsule comprisingpolymers disappearing due to thermal decomposition and carbon precursorpolymers, and baking the aforementioned micro-capsule subsequent tomelting and spinning.

(31) A method of production of a hollow carbon fiber according to aspect(30), characterized by using polymers wherein the residual carbonpercentage of polymers disappearing due to thermal decomposition doesnot exceed 10 percent by weight and that of carbon precursor polymersdoes not exceed 15 percent by weight.

(32) A method of production of a hollow carbon fiber production methodaccording to aspect (30), characterized in the fact that theaforementioned micro-capsules are prepared by an interfacial chemicaltechnique.

(33) A method of production of a hollow carbon fiber according to aspect(30), characterized in the fact that the aforementioned micro-capsulesare prepared by seed polymerization.

(34) A method of production of a hollow carbon fiber production methodaccording to aspect (29), characterized in the fact that theaforementioned carbon precursor polymers are formed of monomerscomprising a radically polymerizable group.

(35) A method of production of a hollow carbon fiber according to aspect(34), characterized in the fact that the aforementioned carbon precursorpolymer has 35 mole percent or more of units formed of acrylonitrilemonomers contained in the polymer.

(36) A method of production of a hollow carbon fiber according to aspect(29), characterized in the fact that the aforementioned polymerdisappearing due to thermal decomposition is formed of a monomercomprising a radically polymerizable group.

(37) A method of production of a hollow carbon fiber according to aspect(29), characterized in the fact that a polymer disappearing due tothermal decomposition and a carbon precursor polymer are formed ofmonomer comprising a radically polymerizable group, and compound whereincarbon remains as a major component in the process of carbonization isused as a polymerization initiator.

(38) A method of production of a hollow carbon fiber according to aspect(29), characterized in the fact that a polymer disappearing due tothermal decomposition and a carbon precursor polymer are formed of amonomer comprising a radically polymerizable group, and a compoundcomprising only an element selected from among carbon, hydrogen, oxygen,nitrogen, phosphorus, sulfur, fluorine, chlorine, bromine and iodine isused as a polymerization initiator.

(39) A composite of the hollow carbon fiber according to aspect (25) anda resin.

(40) A hollow carbon particle comprising a hollow member formed of apolymer disappearing due to thermal decomposition and a carbon shellformed of a carbon precursor polymer.

(41) A method of production of a hollow carbon particle, characterizedin that the aforementioned hollow carbon fiber is produced by acombination of polymers disappearing due to thermal decomposition andcarbon precursor polymers.

(42) A method of production of a hollow carbon particle according toaspect (41), characterized by a step of producing a micro-capsulecomprising polymers disappearing due to thermal decomposition and carbonprecursor polymers, and baking the aforementioned micro-capsule.

(43) A method of production of a hollow carbon particle according toaspects (41) or (42) characterized by using polymers wherein theresidual carbon percentage of polymers disappearing due to thermaldecomposition does not exceed 10 percent by weight and that of carbonprecursor polymers does not exceed 15 percent by weight.

(44) A method of production of a hollow carbon particle according toaspect (42), characterized in the fact that the aforementionedmicro-capsules are prepared by an interfacial chemical technique.

(45) A method of production of a hollow carbon particle according toaspect (42), characterized in the fact that the aforementionedmicro-capsules are prepared by seed polymerization.

(46) A method of production of a hollow carbon particle according toaspect (42), characterized in the fact that the aforementioned carbonprecursor polymers are formed of monomers comprising a radicallypolymerizable group.

(47) A method of production of a hollow carbon particle according toaspect (46), characterized in the fact that the aforementioned carbonprecursor polymer has 35 mole percent or more of units formed ofacrylonitrile monomers contained in polymers.

(48) A method of production of a hollow carbon particle according toaspect (42), characterized in the fact that the aforementioned polymerdisappearing due to thermal decomposition is formed of a monomercomprising a radically polymerizable group.

(49) A method of production of a hollow carbon particle according toaspect (42), characterized in the fact that a polymer disappearing dueto thermal decomposition and a carbon precursor polymer are formed ofmonomer comprising a radically polymerizable group, and compoundcomprising only an element selected from among carbon, hydrogen, oxygen,nitrogen, phosphorus, sulfur, fluorine, chlorine, bromine and iodine isused as a polymerization initiator.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a cross sectional view representing an example of an electrondischarge device wherein a hollow carbon fiber is used as an electrondischarge source;

FIG. 2 is a cross-sectional view representing an example of anequivalent circuit of an electron discharge element where the hollowcarbon fiber, based on a printing method, is used as an electrondischarge source; and

FIG. 3 is a process flow diagram illustrating the hollow carbon fiberproduction process of the present invention.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

The following description is directed to a hollow carbon fiber and itsproduction method, which contains a step of baking and carbonization ofpolymer particles having a specified volume after deforming.

When polymer particles are deformed by heating, they are preferablyheated at a temperature higher than that where they are softened.Further, the heating temperature is preferably higher than the glasstransition temperature.

Although the diameter of the polymer particle is not restricted, thediameter of the carbon fiber as a final product can be controlled interms of the diameter of the polymer particle. Accordingly, use ofpolymer particles having a smaller diameter is preferred to obtainfibers of a small diameter.

It is preferred that the volume of the polymer particle not exceed100mm³. The diameter and length of the carbon fiber as a final productcan be controlled in terms of the volume of the polymer particle. Thus,use of polymer particles having a smaller volume is preferred to obtainfibers of a small diameter.

It is preferable for the aspect ratio (length/diameter) of the fiber tobe 1 or more. Fibers of the optimum aspect ratio can be provided inresponse to the particular application. To obtain fine and long fibers,it is effective to increase the heating temperature, decrease thepolymer viscosity, increase the spinning speed, and increase the windingspeed of the spun yard in the step of melting and spinning.

The difference in the softening temperature between polymersdisappearing due to thermal decomposition forming the polymer particleand carbon precursor polymers preferably is not to exceed 100 degreesCelsius. If the temperature difference exceeds 100 degrees Celsius, adifference in viscosity will occur between the polymer disappearing dueto thermal decomposition and the carbon precursor polymer in the processof spinning, and the spun yarn will tend to break. The difference insoftening temperatures between the two types of aforementioned polymerspreferably is not to exceed 50 degrees Celsius. It is more preferable ifthis difference does not exceed 25 degrees Celsius.

The hollow carbon fiber of the present invention comprises a hollowmember formed of a polymer disappearing due to thermal decomposition atthe time of baking and a carbon shell formed of a carbon precursorpolymer. This can be produced by a combination of polymers disappearingdue to thermal decomposition carbon precursor polymers.

As a specific means, it is preferred to have a step of producing amicro-capture from a polymer disappearing due to thermal decompositionand a carbon precursor polymer, and baking the micro-capsule aftermelting and spinning.

Reaction control in each process will be facilitated by producing amicro-capsule comprising a polymer disappearing due to thermaldecomposition and a carbon precursor polymer, and baking it afterspinning. The present invention makes it easier to control the shape ofthe hollow carbon fiber than the aforementioned known production method,and ensures a higher yield.

In the preparation of a micro-capsule according to the presentinvention, the residual carbon percentage of the polymer disappearingdue to thermal decomposition is preferably equal to or smaller than 15percent by weight, more preferably equal to or smaller than 7 percent byweight, and still more preferably equal to or smaller than 5 percent byweight. The residual carbon percentage of the carbon precursor polymeris preferably equal to or greater than 15 percent by weight, morepreferably equal to or greater than 30 percent by weight, and still morepreferably equal to or greater than 50 percent by weight.

Control of the diameter of the hollow carbon fiber pore and control ofthe structure of the graphite forming the wall are facilitated by theuse of the polymer disappearing due to thermal decomposition, with theresidual carbon percentage being equal to or smaller than 10 percent byweight.

Control of the diameter of the hollow carbon fiber pore and control ofthe structure of the graphite forming the wall will be made difficult bythe use of a carbon precursor polymer having a residual carbonpercentage greater than 15 percent by weight, with the result thatcontrol to obtain a desired shape is made difficult.

If the aforementioned conditions are met, there is no restriction on thematerial used for the micro-capsule in the present invention. When theworkability in the spinning step is taken into account, use of athermoplastic resin is preferred.

For example, olefinic resins, such as polyethylene and polypropylene,diene-based resins, such as polybutadiene, acrylic resins, such asmethyl polyacrylate and ethyl polyacrylate, methacrylic resins, such asmethyl polyamethacrylate and ethyl polymethaacrylate, and polyetherresins, such as vinyl polyacetate resin, polyvinyl alcohol resin,polyethylene glycol, and polypropylene glycol can be enumerated aspreferred materials for the polymer disappearing due to thermaldecomposition

Of these acrylic resins, such as methyl polyacrylate and ethylpolyacrylate and methacrylic resins, such as methyl polymethacrylate andethyl polymethacrylate, are preferred.

Polyacrylonitrile resin, phenol resin, furan resin, divinyl benzeneresin, unsaturated polyester resin, polyimide resin, diallyl phthalateresin, vinyl ester resin, polyurethane resin, melamine resin and urearesin can be enumerated as preferred materials for the carbon precursorpolymer.

No restriction is placed on the production method for the aforementionedmicro-capsule. When the workability in the spinning step is taken intoaccount, use of the following method is preferred: seed polymerizationbased on the seed of a polymer disappearing due to thermal decompositionhaving a diameter of 0.001 to 100 micron (μm), a coacervation method, aninterfacial condensation method, a spray drying method and a wetblending method based on use of a hybridizer. The seed polymerizationmethod is preferred when the polymer disappearing due to thermaldecomposition has a diameter of 0.001 to 1 micron.

When the micro-capsule is synthesized according to the seedpolymerization method, it is preferred to synthesize the micro-capsulefrom the radically polymerizable monomer. Polyacrylonitrile resin usingacrylonitrile resin as a monomer is preferred. Polyacrylonitrile resincontaining 35 mole % or more monomer unit formed by acrylonitrile resinin the polymer is preferred.

No restriction is placed on the production method for the polymerdisappearing due to thermal decomposition having a diameter of 0.001 to100 micron. The following methods can be cited as examples: a method ofscreening for pulverization of a polymer disappearing due to thermaldecomposition, or a method of directly obtaining particles bypolymerization, such as reversed phase emulsion polymerization, emulsionpolymerization, soap free emulsion polymerization, non-aqueousdispersion polymerization, seed polymerization and suspensionpolymerization. A method of directly obtaining particles bypolymerization, such as reversed phase emulsion polymerization, emulsionpolymerization, soap free emulsion polymerization, non-aqueousdispersion polymerization, seed polymerization and suspensionpolymerization, is preferred when the workability is taken into account.Emulsion polymerization and soap free emulsion polymerization arepreferred to obtain the polymer disappearing due to thermaldecomposition having a diameter of 0.001 to 1 micron.

No restriction is placed on the polymerization initiator used whenproducing micro-capsules. When a finally produced hollow carbon fiber ofhigher purity is required, it is preferred to use a compound in whichcarbon remains as a main component in the step of carbonization, forexample, the compound comprising only an element selected from amongcarbon, hydrogen, oxygen, nitrogen, phosphorus, sulfur, fluorine,chlorine, bromine and iodine, wherein the content of the elements otherthan carbon does not exceed 30%. Such a compound is exemplified a bydiazo compound, such as azobisisobutylonitrile, azobis (2-aminopropane)dihydrochloride, azobis-4-cyianopentanoic acid andazobisdimethylvaleronitrile, organic peroxide, such as benzoyl peroxide,and peroxide salt, such as ammonium persulfate.

The micro-capsule obtained from the aforementioned step is fed to thespinning step. There is no restriction on the spinning means accordingto the present invention; accordingly, a known method can be used.

For example, when the micro-capsule is molten, it is put into acopper-made crucible as a material together with the resin becoming amatrix (for example, a polymer disappearing due to thermal decompositionwhich is the same one as that used as the aforementioned micro-capsuleseed or a different one), and is heated to 100 to 300 degrees Celsius bya ribbon heater until the material is molten. Then, the molten resinmaterial is wound by a motor through a pore (e.g. 1 mm in diameter).

In this case, there is no restriction to the blending ratio between themicro-capsule and a matrix. For example, the ratio of the former to thelatter is preferably 1 to 0.3 through 1.5. The form of the hollow carbonfiber can be controlled by adjusting the heating temperature at the timeof melting the material, the pore diameter on the bottom of thecrucible, the speed of the winding motor, and the peripheral speed andshape of the winding portion.

Then, a hollow carbon fiber can be obtained in the step of baking andcarbonization. The baking and carbonization temperature is preferablyfrom 500 to 3200 degrees Celsius, and, more preferably, from 600 to 3000degrees Celsius. If the baking and carbonization temperature is below500 degrees Celsius, formation of a graphite layer will be insufficient,with the result that such characteristics as the mechanical strength,the hydrogen storage characteristics and the electric field dischargecharacteristics will be reduced. If the baking and carbonizationtemperature is higher than 3200 500 degrees Celsius, part or almost allof the carbon atoms forming a graphite layer will subliminate, with theresult that a defect will be caused on the graphite layer.

The hollow carbon fiber obtained in the aforementioned step ischaracterized in that the content of metal and a metallic compound is 1percent by weight or less.

The production method according to the present invention allows hollowcarbon fibers to be produced without using a metal or a metalliccompound in the hollow carbon fiber production process, or withoutremoving or refining metal or a metallic compound wherein the content ofmetal and metallic compound is 1 percent by weight or less.

The conventional method for producing a carbon fiber requires a catalystof metal and a metallic compound for the purpose of growth of a gasphase especially in the step of producing carbon tubes. The presentinvention, however, provides carbon fibers of high purity, especiallycarbon nano-tubes of high purity, without requiring any catalyst ofmetal or a metallic compound in a step of the production; hence, no stepof removing and refining the catalyst of metal and a metallic compoundafter production is required.

The following description is directed to a specific production methodaccording to the present invention. However, the present invention isnot restricted thereto. For example, it is also possible to form ahollow member using a polymer disappearing due to thermal decompositionin the step of baking, and to form a shell using a carbon precursorpolymer, which is turned into carbon by baking. Namely, production isbased on a combination between the polymer disappearing due to thethermal decomposition and a carbon precursor polymer.

To put it more specifically, the preferred method for producing hollowcarbon fibers is to form micro-capsules from the polymer disappearingdue to thermal decomposition and a carbon precursor polymer and to bakethem subsequent to melting and spinning.

Reaction control in each process will be facilitated by producing amicro-capsule comprising a polymer disappearing due to thermaldecomposition and a carbon precursor polymer, and baking it afterspinning. The present invention makes it easier to control the shape ofthe hollow carbon fiber than the aforementioned known production method,and ensures a higher yield.

The following description is directed to embodiments according to thepresent invention:

First Embodiment

(1) Synthesis of a Polymer Disappearing Due to Thermal Decomposition

35 ml of methyl methacrylate, 350 ml of ion exchange water and 29 mgammonium persulfate were put in a 1000 ml flask, and an ultrasonic wavewas applied for 30 minutes while nitrogen was bubbling therein. Anagitating blade was mounted on the flask, and a reaction was performedby agitating it at a speed of 300 rpm at 70 degrees Celsius for 5 hours,then at 80 degrees Celsius for 30 minutes. An emulsified polymersolution disappearing due to thermal decomposition was obtained by thisstep.

(2) Preparation of Micro-capsules

90 ml of emulsified polymer solution disappearing due to thermaldecomposition obtained in step (1), 4 ml of acrylonitrile (carbonprecursor polymer), 270 ml of ion exchange water and 5 mg ammoniumpersulfate were sampled and placed in a 1000 ml flask. Nitrogen gas wasbubbled in the aforementioned flask for 30 minutes. Then, an agitatingblade was mounted on the flask, and a reaction was performed byagitating it at a speed of 300 rpm at 70 degrees Celsius for 5 hours,then at 80 degrees Celsius for 30 minutes. An emulsified micro-capsulesolution was obtained by this step. Water was removed from thisemulsified micro-capsule solution by freezing and drying to getmicro-capsules.

(3) Spinning, Baking and Carbonization of Micro-capsules

After the micro-capsule obtained in step (2) and the pulverized powderof resin disappearing due to thermal decomposition obtained in step (1)were blended in a mortar at a ratio of 1 to 1 (in weight percentage),they were kneaded while being heated at 120 degrees Celsius in anitrogen atmosphere, thereby obtaining a resin lump.

Then, this resin lump was put into a copper-made crucible having adiameter of 30 mm and a length of 100 mm with a 1 mm-diameter pore onthe bottom. In the nitrogen atmosphere, this copper-made crucible washeated to 170 degrees Celsius by a ribbon heater. Through the pore onthe bottom of the copper-made crucible, molten resin was wound on amotor driven at a peripheral speed of 50 m/min., thereby allowing theaforementioned resin lump to be spun.

The fiber gained in the aforementioned spinning step was subjected tomelt-proofing in an air flow rate of 30 ml/min. Then, it was heated andbaked up to 1000 degrees Celsius at a temperature rising speed of 10degrees Celsius/hour in an atmosphere of flowing nitrogen in a bakingkiln. Then, it was heated by a Tammann electric furnace up to 3000degrees Celsius at a temperature rising speed of 30 degreesCelsius/hour, and was subjected to graphitization.

The carbon fiber obtained in the aforementioned step was a hollow carbonfiber consisting of three to scores of graphite layers constituting a3-to 12-nm diameter wall having a pore diameter of 1 to 3 nm.

The amount of metal and metallic compound in the obtained hollow fiberwas measured according to procedures specified in the JapaneseIndustrial Standards graphite ash measuring procedure to obtain thevalue of 0.01 wt %.

(4) Composite Preparation Method

The hollow carbon fiber obtained in the aforementioned step was used asa filler and was combined with epoxy resin to form a composite. Thiscomposite was characterized by excellent properties, such as lightweight, superb strength and high resistance to heat. It was very usefulfor various types of structural members.

Second Embodiment

(1) Synthesis of Resin Disappearing Due to Thermal Decomposition

35 ml of methyl methacrylate, 350 ml of ion exchange water and 29 gm ofammonium persulfate were put in a 1000 ml flask, and an ultrasonic wavewas applied for 30 minutes while nitrogen was bubbling therein. Anagitating blade was mounted on the flask, and a reaction was performedby agitating it at a speed of 300 rpm at 70 degrees Celsius for 5 hours,then at 80 degrees Celsius for 30 minutes. An emulsified polymersolution disappearing due to thermal decomposition was obtained by thisstep.

(2) Preparation of Micro-capsules From a Polymer Disappearing Due toThermal Decomposition and a Carbon Precursor Polymer

90 ml of emulsified polymer solution disappearing due to thermaldecomposition obtained in step (1), 4 ml of acrylonitrile, 270 ml of ionexchange water and 5 mg of ammonium persulfate were placed in a 1000 mlflask. Nitrogen gas was bubbled for 30 minutes. Then, an agitating bladewas mounted on the flask, and a reaction was performed by agitating itat a speed of 300 rpm at 70 degrees Celsius for 5 hours, then at 80degrees Celsius for 30 minutes. An emulsified micro-capsule solution wasobtained by this step. Water was removed from this emulsifiedmicro-capsule solution by freezing and drying to obtain micro-capsules.

(3) Carbonization of Micro-capsules

The micro-capsule obtained in step (2) was subjected to melt-proofing inan air flow rate of 30 ml/min. Then, it was heated and baked up to 1000degrees Celsius at a temperature rising speed of 10 degrees Celsius/hourin the atmosphere of flowing nitrogen. Then, it was heated by a Tammannelectric furnace up to 3000 degrees Celsius at a temperature risingspeed of 30 degrees Celsius/hour and was subjected to graphitization.

The carbon fiber obtained in the aforementioned step was a hollow carbonfiber consisting of three to scores of graphite layers constituting a 5to 50-nm diameter wall having a pore diameter of 3 to 30 nm.

Third Embodiment Adjustment of Polymer Disappearing Due to ThermalDecomposition Including Metallic Complex

35 g of methyl methacrylate, 2 mg of bis(acetylacetone) platinum, 320 gof azobisisobutylonitrile, 350 ml of ion exchange water and 1.0 g ofpolyvinyl alcohol were made to react in a 1000 ml flask at a temperatureof 80 degrees Celsius for 8 hours. Particles were collected byfiltering, and were washed in water and dried to obtain polymerparticles disappearing due to thermal decomposition having an averageparticle diameter of about 200 microns including platinum.

Preparation of Micro-capsules

50 g of the polymer particles prepared in the above step and 25 g ofphenol resin having a particle diameter of 50 microns were treated by ahybridizer to obtain micro-capsules, where polymethyl methacrylateincluding a platinum complex was used as a core and phenol resin wasused as a shell.

Spinning and Carbonization of Micro-capsule

The micro-capsule prepared in the above step and pulverized polymerdisappearing due to thermal decomposition including platinum prepared inthe above step were slightly mixed at a ratio of 1 to 1 in weightpercentage in a mortar. Then, they were kneaded while being heated at120 degrees Celsius in a nitrogen atmosphere, thereby obtaining a resinlump. Then, this resin lump was put into a copper-made crucible having adiameter of 30 mm and a length of 100 mm with a 1 mm-diameter pore onthe bottom. In a nitrogen atmosphere, this copper-made crucible washeated to 170 degrees Celsius by a ribbon heater. Through the pore onthe bottom of the copper-made crucible, molten resin was wound on amotor driven at a peripheral speed of 50 meters, thereby allowing theaforementioned resin lump to be spun.

The fiber gained by spinning was cut into 1 mm pieces, and was thensubjected to melt-proofing in an air flow rate of 30 ml/min. Then, itwas baked up to 1000 degrees Celsius at a temperature rising speed of 10degrees Celsius/hour in an atmosphere of flowing nitrogen in a bakingkiln. Then, it was heated by a Tammann electric furnace up to 3000degrees Celsius at a temperature rising speed of 30 degrees Celsius/hourand was subjected to graphitization.

The obtained carbon fiber was examined by a transmission electronmicroscope to find out that it had a diameter of 3 to 12 nm with a porediameter from 1 to 3 nm. Further, 70% of the examined samples had adiameter from 8 to 12 nm. It was found to be a hollow carbon fiberconsisting of three to scores of graphite layers constituting the wallthereof.

1 g of this hollow fiber was put into a magnetic crucible having aninner volume of 5 ml. It was subjected to ash treatment at 600 degreesCelsius in an atmosphere of air for three hours. Ash was molten togetherwith 20 g of sodium peroxide and was dissolved in chloroazotic acid toobtain a solution. The concentration of platinum in this solution wasmeasured and found to be 0.10%.

Electron Discharge Characteristics of an Electron Discharge DeviceWherein a Hollow Carbon Fiber is Used as an Electron Discharge Source

Paste using the aforementioned hollow carbon fiber was prepared. Thepaste was made up of 1 part by weight of hollow carbon fibers dispersedover 2 parts by weight of butyl Carbitol acetate and 0.2 part by weightof ethyl cellulose.

This paste was used to create a cathode substrate having a structureserving as a basis for FIG. 1. Namely, a 5 mm square cathode electrodewas formed by pattern printing and baking of a silver paste on aborosilicate glass substrate. The aforementioned 6 mm square carbonfiber paste was printed so as to cover this cathode electrode, and itwas baked at 550 degrees Celsius in air to obtain a hollow carbon fiberfilm. Fifty microns above this simple electrode, a stainless steel diskhaving a diameter of 1 mm was placed as an anode face-to-face with itvia a spacer.

This cathode and anode were set into a vacuum device to obtain a vacuumof 1×10 (0.5) Pa by evacuation.

A voltage was applied between the cathode and anode, and the currentdischarged from the cathode was measured to verify the voltage where anelectron discharge current started to occur. It was revealed that thelimit of the current measurement was 1×10(0.7) amperes. When a voltageof 65 volts was applied, the measurement limit of 1×10(0.7) amperes wasobserved.

Fourth Embodiment Preparation of Emulsified Polymer SolutionDisappearing Due to Thermal Decomposition Without Metallic Complex

“2 mg of bis(acetylacetone) platinum” in the preparation of emulsifiedan polymer solution disappearing due to thermal decomposition in theFirst Embodiment was changed to “0 mg of bis(acetylacetone) platinum”.Otherwise, the present embodiment is the same as the First Embodiment.Based on this condition, polymer particles disappearing due to thermaldecomposition without metallic complex were prepared.

Preparation of Carbon Precursor Without Metallic Complex

50 g of polymer particles disappearing due to thermal decompositionwithout metallic complex as prepared in the aforementioned step and 25 gof phenol resin particles having a particle diameter of 5 microns weretreated by a hybridizer to obtain micro-capsules without metalliccomplex, where polymethyl methacrylate was used as a core and phenolresin was used as a shell.

Treatment of the Metallic Complex Deposited on the Outside ofMicro-capsules, Spinning and Carbonization

Micro-capsules without metallic complex prepared in the aforementionedstep and polymer particles disappearing due to thermal decomposition,including platinum prepared in Embodiment 1, were slightly mixed at aratio of 1 to 1 in weight percentage in a mortar.

Then, they were kneaded while being heated at 120 degrees Celsius in anitrogen atmosphere, thereby obtaining a resin lump. Then this resinlump was subjected to a treatment of spinning, melt-proofing, baking andgraphitization in a manner similar to that of the first Embodiment.

The obtained carbon fiber was examined by a transmission electronmicroscope, and it was found to have a diameter of 3 to 12 nm with apore diameter from 1 to 3 nm. Further, 70% of the examined samples had adiameter from 8 to 12 nm. It was a hollow carbon fiber consisting ofthree to scores of graphite layers constituting the wall thereof.

Similarly to the First Embodiment, this hollow carbon fiber wassubjected to ashing treatment, and the platinum concentration was foundto be 0.06% according to the ICP measurement.

Electron Discharge Characteristics of an Electron Discharge DeviceWherein a Hollow Carbon Fiber is Used as an Electron Discharge Source

According to the same measuring method as that of the First Embodiment,the aforementioned hollow carbon fiber was used to measure the currentdischarged from the cathode when voltage was applied between the cathodeand anode. As a result, a measurement limit of 1×10(0.7) amperes wasobserved when a voltage of 75 volts was applied.

Comparative Example 1 Preparation of Emulsified Polymer SolutionDisappearing Due to Thermal Decomposition Without Metallic Complex

“2 mg of bis (acetylacetone) platinum” in the preparation of emulsifiedpolymer solution disappearing due to thermal decomposition in the FirstEmbodiment was changed to “0 mg of bis(acetylacetone) platinum”.Otherwise, the present embodiment is the same as the First Embodiment.Based on this condition, polymer particles disappearing due to thermaldecomposition without metallic complex were prepared.

Preparation of Carbon Precursor Without Metallic Complex

Carbon precursor without metallic complex was prepared under the samecondition as that of the First Embodiment, except that 90 g of theaforementioned emulsified polymer solution disappearing due to thermaldecomposition without metallic complex as a polymer disappearing due tothermal decomposition was used.

Spinning and Carbonization of Micro-capsules Without Metallic Capsule

Carbon fibers without metallic capsule were produced under the samecondition as that of the First Embodiment, except that theaforementioned micro-capsules without metallic capsule were used asmetallic capsules, and the pulverized polymer prepared by freezing anddrying the aforementioned emulsified polymer solution disappearing dueto thermal decomposition without metallic complex to remove water wasused as a pulverized polymer disappearing due to thermal decomposition.

The obtained carbon fiber was examined by a transmission electronmicroscope, and it was found to have a diameter of 3 to 12 nm with apore diameter from 1 to 3 nm. Further, 70% of the examined samples had adiameter from 8 to 12 nm. It was a hollow carbon fiber consisting ofthree to scores of graphite layers constituting the wall thereof.

Electron Discharge Characteristics of an Electron Discharge DeviceWherein a Hollow Carbon Fiber Without Metallic Complex is Used as anElectron Discharge Source

According to the same measuring method as that of the First Embodiment,the aforementioned hollow carbon fiber was used to measure the currentdischarged from the cathode when a voltage was applied between thecathode and anode. As a result, a measurement limit of 1×10(0.7) ampereswas observed when a voltage of 800 volts was applied.

The voltage applied when the measurement limit current is observed isextremely high, and the electric resistance is also high in ComparativeExample 1, as compared with the First and Second Embodiments where thehollow carbon fiber including the metallic complex is used. In thisrespect, the electron discharge characteristics are poorer inComparative Example 1.

Hollow carbon fibers and hollow carbon particles according to thepresent invention hardly contain metal or a metallic compound, or do notcontain it at all. Hence, they are free from various contaminations dueto metal or unstable electric discharge and can be used in a greatvariety of fields.

The method of producing hollow carbon fibers according to the presentinvention makes it possible to control hollow carbon fibers representedby carbon tubes with respect to their characteristic shape, fiberdiameter, fiber lengths, pore diameter, thickness of the wall-forminggraphite layer, crystallinity and the like.

No metallic catalyst is used in the process of producing hollow carbonfibers and hollow carbon particles; hence, no refining is required. Thepresent invention allows hollow carbon fibers and hollow carbonparticles of a desired shape to be produced at a high yield rate.

Hollow carbon fibers and hollow carbon particles according to thepresent invention provide composites characterized by excellentproperties, such as light weight, superb strength and high resistance toheat.

The present invention allows the particle diameter, pore diameter andwall to be determined by adjusting hollow carbon particles representedby fullerene.

What is claimed is:
 1. A hollow carbon fiber production methodcomprising a step of baking and carbonizing polymer particles having avolume of 100 mm³ or smaller after deforming.
 2. A hollow carbon fiberproduction method according to claim 1, wherein the polymer particlesare deformed by heat.
 3. A hollow carbon fiber production methodaccording to claim 1, wherein the polymer particles are deformed bymechanical force.
 4. A hollow carbon fiber production method accordingto claim 1, wherein the polymer particles are deformed by irradiation ofelectromagnetic wave.
 5. A hollow carbon fiber production methodaccording to claim 1, wherein the polymer particles are deformed by acombination of at least two of heat, mechanical force and irradiationwith electromagnetic waves.
 6. A hollow carbon fiber production methodaccording to claim 1, characterized in that the diameter of the polymerparticles is 5 to 5000 times that of a hollow carbon fiber as a finalproduct.
 7. A hollow carbon fiber production method according to claim1, wherein one or both ends of the fiber are closed.
 8. A hollow carbonfiber production method according to claim 1, wherein an aspect ratio(length/diameter) of the fiber is 1 or more.
 9. A hollow carbon fiberproduction method according to claim 1, wherein a diameter and length ofa fiber are controlled by volume of the polymer particles.
 10. A hollowcarbon fiber production method according to claim 1, comprising a stepof producing the polymer particles by a combination of polymersdisappearing due to thermal decomposition and carbon precursor polymers.11. A hollow carbon fiber production method according to claim 10,comprising a step of producing micro-capsules from the polymersdisappearing due to thermal decomposition and the carbon precursorpolymers, and baking said micro-capsules subsequent to melting andspinning.
 12. A hollow carbon fiber production method according to claim11, wherein a ratio between inner and outer diameters of said hollowcarbon fiber is controlled by a ratio of thickness between a layer ofpolymers disappearing due to thermal decomposition and that of thecarbon precursor polymers.
 13. A hollow carbon fiber production methodaccording to claim 11, wherein a number of layers of said hollow carbonfiber is controlled by a ratio of thickness between a layer of polymersdisappearing due to thermal decomposition and that of the carbonprecursor polymers.
 14. A hollow carbon fiber production methodaccording to claim 11, wherein a residual carbon percentage of thepolymer disappearing due to thermal decomposition does not exceed 10percent by weight and that of the carbon precursor polymers does notexceed 15 percent by weight.
 15. A hollow carbon fiber production methodaccording to claim 11, wherein said micro-capsules are prepared by aninterfacial chemical technique.
 16. A hollow carbon fiber productionmethod according to claim 11, wherein said micro-capsules are preparedby seed polymerization.
 17. A hollow carbon fiber production methodaccording to claim 11, wherein said carbon precursor polymers are formedof monomer comprising radically polymerizable groups.
 18. A hollowcarbon fiber production method according to claim 17, wherein saidcarbon precursor polymers have units formed of acrylonitrile monomerscontained in polymers.
 19. A hollow carbon fiber production methodaccording to claim 11, wherein said polymers disappearing due to thermaldecomposition are formed of a monomer comprising a radicallypolymerizable group.
 20. A hollow carbon fiber production methodaccording to claim 11, wherein the polymers disappearing due to thermaldecomposition and the carbon precursor polymers are formed of a monomercomprising radically polymerizable groups, and a compound wherein carbonremains as a major component in the process of carbonization is used asa polymerization initiator.
 21. A hollow carbon fiber production methodaccording to claim 10, wherein a difference between softeningtemperature of the polymers disappearing due to thermal decompositionand that of the carbon precursor polymers does not exceed 100 degreesCelsius.
 22. A hollow carbon fiber production method according to claim10, wherein a ratio between inner and outer diameters of said hollowcarbon fiber is controlled by a ratio of thickness between a layer ofpolymers disappearing due to thermal decomposition and that of thecarbon precursor polymers.
 23. A hollow carbon fiber production methodaccording to claim 10, wherein a number of layers of said hollow carbonfiber is controlled by a ratio of thickness between a layer of polymersdisappearing due to thermal decomposition and that of the carbonprecursor polymers.
 24. A hollow carbon fiber production methodaccording to claim 10, wherein a residual carbon percentage of thepolymer disappearing due to thermal decomposition does not exceed 10percent by weight and that of the carbon precursor polymers does notexceed 15 percent by weight.
 25. A hollow carbon fiber according toclaim 1, wherein each of the polymer particles has a prescribed volume.26. A hollow carbon fiber according to claim 25, comprising a hollowcarbon fiber formed of polymer disappearing due to thermal decompositionand a carbon shell formed of carbon precursor polymer.
 27. A hollowcarbon fiber according to claim 1, comprising a hollow carbon fiberformed of polymer disappearing due to thermal decomposition and a carbonshell formed of carbon precursor polymer.
 28. A composite of the hollowcarbon fiber according to claim 27 and resin.